GNA11 + GNAQ antibody [HL2203]

GNA11 + GNAQ antibody [HL2203] detects GNA11 + GNAQ protein by immunofluorescent analysis.
Sample: MDCK cells were fixed in ice-cold MeOH for 5 min.
Green: GNA11 + GNAQ stained by GNA11 + GNAQ antibody [HL2203] (GTX638207) diluted at 1:500.
Red: alpha Tubulin, a cytoskeleton marker, stained by alpha Tubulin antibody [GT114] (GTX628802) diluted at 1:1000.
Blue: Fluoroshield with DAPI (GTX30920).

Whole cell extract (30 μg) was separated by 10% SDS-PAGE, and the membrane was blotted with GNA11 + GNAQ antibody [HL2203] (GTX638207) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Various cell extracts (30 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with GNA11 + GNAQ antibody [HL2203] (GTX638207) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Whole cell extract (30 μg) was separated by 10% SDS-PAGE, and the membrane was blotted with GNA11 + GNAQ antibody [HL2203] (GTX638207) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 10% SDS-PAGE, and the membrane was blotted with GNA11 + GNAQ antibody [HL2203] (GTX638207) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Whole cell extract (30 μg) was separated by 10% SDS-PAGE, and the membrane was blotted with GNA11 + GNAQ antibody [HL2203] (GTX638207) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.